Günther S, Piwon N, Iwanska A, Schilling R, Meisel H, Will H
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie an der Universität Hamburg, Federal Republic of Germany.
J Virol. 1996 Dec;70(12):8318-31. doi: 10.1128/JVI.70.12.8318-8331.1996.
Little is known about the functional significance of hepatitis B virus (HBV) sequence heterogeneity. Here we analyzed the type, frequency, and function of mutations in the core promoter/enhancer II region of HBV in immunosuppressed patients. The major HBV population in immunosuppressed patients with severe liver disease had deletions, insertions, and/or base changes in this region. Such mutations were not found in immunosuppressed patients with mild disease. Except for two mutations, all created a hepatocyte nuclear factor 1 (HNF1) binding site or a potential HNF3 binding site. Occasionally, known binding sites for C/EBP and HNF4 were additionally duplicated. Eleven mutated core promoter prototype sequences were functionally tested in the context of a wild-type genome by transfection in Huh7 cells. Despite the diversity of mutations tested, all decreased steady-state levels of pre-C mRNA drastically and increased those of the C mRNA/ pregenomic RNA. This correlated with reduced levels of secreted hepatitis B e antigen and increased intracellular levels of core and Pol proteins and replicative HBV DNA intermediates. The levels of secreted HBV DNA-containing particles were also increased although most of the mutations reduced the levels of pre-S/S mRNA and pre-S1, and pre-S2 proteins as well as secretion of hepatitis B surface antigen. These data reveal a novel class of HBV variants with HNF1 binding sites in the core promoter which are characterized by a defect in hepatitis B e antigen expression, enhanced replication, and altered protein levels, all probably mediated by altered transcription factor binding. The phenotype of these variants and their prevalence only in immunosuppressed patients with severe liver disease may indicate that they play a role in pathogenesis.
关于乙型肝炎病毒(HBV)序列异质性的功能意义,人们了解甚少。在此,我们分析了免疫抑制患者中HBV核心启动子/增强子II区域突变的类型、频率和功能。患有严重肝病的免疫抑制患者中的主要HBV群体在该区域存在缺失、插入和/或碱基变化。在患有轻度疾病的免疫抑制患者中未发现此类突变。除了两个突变外,所有突变均产生了一个肝细胞核因子1(HNF1)结合位点或一个潜在的HNF3结合位点。偶尔,已知的C/EBP和HNF4结合位点会额外重复。通过在Huh7细胞中进行转染,在野生型基因组背景下对11个突变的核心启动子原型序列进行了功能测试。尽管所测试的突变具有多样性,但所有突变均大幅降低了前C mRNA的稳态水平,并提高了C mRNA/前基因组RNA的稳态水平。这与分泌型乙型肝炎e抗原水平降低以及核心蛋白、Pol蛋白和复制性HBV DNA中间体的细胞内水平升高相关。尽管大多数突变降低了前S/S mRNA、前S1和前S2蛋白的水平以及乙型肝炎表面抗原的分泌,但含HBV DNA颗粒的分泌水平也有所增加。这些数据揭示了一类新型的HBV变体,其核心启动子中具有HNF1结合位点,其特征为乙型肝炎e抗原表达缺陷、复制增强和蛋白水平改变,所有这些可能都是由转录因子结合改变介导的。这些变体的表型及其仅在患有严重肝病的免疫抑制患者中的流行情况可能表明它们在发病机制中起作用。